KR900014405A - 세팔로스포린 유도체 및 이의 제조방법 - Google Patents
세팔로스포린 유도체 및 이의 제조방법 Download PDFInfo
- Publication number
- KR900014405A KR900014405A KR1019900004083A KR900004083A KR900014405A KR 900014405 A KR900014405 A KR 900014405A KR 1019900004083 A KR1019900004083 A KR 1019900004083A KR 900004083 A KR900004083 A KR 900004083A KR 900014405 A KR900014405 A KR 900014405A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- methyl
- compound
- group
- cepem
- Prior art date
Links
- 229930186147 Cephalosporin Natural products 0.000 title 1
- 229940124587 cephalosporin Drugs 0.000 title 1
- 150000001780 cephalosporins Chemical class 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- -1 2-aminothiazol-4-yl Chemical group 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 7
- 150000002148 esters Chemical class 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 208000035143 Bacterial infection Diseases 0.000 claims 3
- 208000022362 bacterial infectious disease Diseases 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 230000004913 activation Effects 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
- C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (9)
- 일반식(I)의 세펨카복실산 에스테르 또는 생리학적으로 허용되는 이의 산부가염.상기식에서, R1은 수소 또는 메틸이고, R2는 메틸 또는 에틸이며, HO 그룹은 syn-위치로 존재한다.
- 2, 2-디메틸프로파노일-옥시메틸-7-〔2-(2-아미노티아졸-4-일)-2-(Z)-하이드록시이미노-아세트아미도〕-3-(2-메톡시에톡시-메틸)-3-세펨-4-카복실레이트.
- 2, 2-디메틸프로파노일-옥시메틸 7-〔2-(2-아미노티아졸-4-일)-2-(Z)-하이드록시이미노-아세트아미도〕-3-(2-메톡시에톡시-메틸)-3-세펨-4-카복실레이트.
- α-(2, 2-디메틸프로파노일-옥시)에틸 7-〔2-(2-아미노티아졸-4-일)-2-(Z)-하이드록시이미노-아세트아미도〕-3-(2-메톡시에톡시-메틸)-3-세펨-4-카복실레이트.
- α-(2, 2-디메틸프로파노일-옥시)에틸 7-〔2-(2-아미노티아졸-4-일)-2-(Z)-하이드록시이미노-아세트아미도〕-3-(2-메톡시에톡시-메틸)-3-세펨-4-카복실레이트.
- a) 일반식(II)의 화합물을 일반식(III)의 화합물과 반응시켜서 일반식(IV)의 에스테르를 수득하여 자체 공지된 방법으로 그룹 R3및 R4를 제거하거나, b) 일반식(IV)의 화합물을 일반식(VI)의 화합물 또는 이 화합물의 염과 반응시켜서 일반식(IV)의 화합물을 수득하여 자체 공지된 방법으로 그룹 R3및 R4를 분해 제거하거나, c) 일반식(VII)의 화합물을 티오우레아와 반응시켜서 일반식(I),의 화합물을 수득하고, 경우에 따라 수득된 화합물을생리학적으로 허용되는 산부가염으로 전환시킴을 특징으로 하여, 일반식(I)의 세펨카복실산 에스테르 또는 생리학적으로 허용되는 이의 산부가염을 제조하는 방법.상기식에서, R1은 수소 또는 메틸이고, R2는 메틸 또는 에틸이며, HO 그룹은 syn-위치로 존재하고, R3는 아미노-보호 그룹이며, R4는 쉽게 분해 제거할 수 있는 그룹이고, A는 양이온이며, X는 이탈 그룹이고, Y는 활성화 그룹이며, Z는 할로겐이다.
- 일반식(I)의 세펨카복실산 에스테르를 함유하는, 세균성 감염에 대해 치료 활성인 약제학적 제제.
- 일반식(I)의 세펨카복실산 에스테르를 약제학적으로 통상적인 부형제 또는 희석제를 사용하여 약제학적으로 적당한 투여 형태로 제조함을 특징으로 하여, 세균성 감염에 대해 치료활성인 약제학적 제제를 제조하는 방법.
- 세균성 감염을 치료하기 위한 일반식(I)의 세펨 카복실산 에스테르의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3910093.6 | 1989-03-29 | ||
DEP3910093.6 | 1989-03-29 | ||
DE3910093A DE3910093A1 (de) | 1989-03-29 | 1989-03-29 | Cephalosporinderivate und verfahren zu ihrer herstellung |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900014405A true KR900014405A (ko) | 1990-10-23 |
KR0164433B1 KR0164433B1 (ko) | 1999-01-15 |
Family
ID=6377347
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900004083A KR0164433B1 (ko) | 1989-03-29 | 1990-03-27 | 세팔로스포린 유도체 및 이의 제조방법 |
Country Status (17)
Country | Link |
---|---|
US (1) | US5306717A (ko) |
EP (1) | EP0390066B1 (ko) |
JP (1) | JP2898054B2 (ko) |
KR (1) | KR0164433B1 (ko) |
AT (1) | ATE143963T1 (ko) |
AU (1) | AU619395B2 (ko) |
CA (1) | CA2013226C (ko) |
DE (2) | DE3910093A1 (ko) |
DK (1) | DK0390066T3 (ko) |
ES (1) | ES2094734T3 (ko) |
FI (1) | FI93015C (ko) |
GR (1) | GR3021531T3 (ko) |
HU (1) | HU205122B (ko) |
IL (1) | IL93908A (ko) |
NO (1) | NO901418L (ko) |
PT (1) | PT93581B (ko) |
ZA (1) | ZA902381B (ko) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0531875T3 (da) * | 1991-09-07 | 2004-06-21 | Aventis Pharma Gmbh | Diastereomer af 3-cephem-4-carboxylsyre-1-(-isopropoxycarbonyloxy)-ethylester og fremgangsmåde til dens fremstilling |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2714880A1 (de) * | 1977-04-02 | 1978-10-26 | Hoechst Ag | Cephemderivate und verfahren zu ihrer herstellung |
FR2476087A1 (fr) * | 1980-02-18 | 1981-08-21 | Roussel Uclaf | Nouvelles oximes derivees de l'acide 3-alkyloxy ou 3-alkyl-thiomethyl 7-amino thiazolyl acetamido cephalosporanique, leur procede de preparation et leur application comme medicaments |
JPS5759894A (en) * | 1980-09-30 | 1982-04-10 | Sankyo Co Ltd | Cephalosporin for oral administration |
-
1989
- 1989-03-29 DE DE3910093A patent/DE3910093A1/de not_active Withdrawn
-
1990
- 1990-03-27 KR KR1019900004083A patent/KR0164433B1/ko not_active IP Right Cessation
- 1990-03-27 FI FI901520A patent/FI93015C/fi active IP Right Grant
- 1990-03-27 DK DK90105798.4T patent/DK0390066T3/da active
- 1990-03-27 IL IL9390890A patent/IL93908A/en not_active IP Right Cessation
- 1990-03-27 ES ES90105798T patent/ES2094734T3/es not_active Expired - Lifetime
- 1990-03-27 EP EP90105798A patent/EP0390066B1/de not_active Expired - Lifetime
- 1990-03-27 DE DE59010527T patent/DE59010527D1/de not_active Expired - Lifetime
- 1990-03-27 AT AT90105798T patent/ATE143963T1/de not_active IP Right Cessation
- 1990-03-28 NO NO90901418A patent/NO901418L/no unknown
- 1990-03-28 PT PT93581A patent/PT93581B/pt not_active IP Right Cessation
- 1990-03-28 AU AU52324/90A patent/AU619395B2/en not_active Expired
- 1990-03-28 ZA ZA902381A patent/ZA902381B/xx unknown
- 1990-03-28 CA CA002013226A patent/CA2013226C/en not_active Expired - Lifetime
- 1990-03-29 JP JP2082885A patent/JP2898054B2/ja not_active Expired - Lifetime
- 1990-03-29 HU HU901893A patent/HU205122B/hu unknown
-
1992
- 1992-07-24 US US07/924,598 patent/US5306717A/en not_active Expired - Lifetime
-
1996
- 1996-10-31 GR GR960402900T patent/GR3021531T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
PT93581B (pt) | 1996-03-29 |
KR0164433B1 (ko) | 1999-01-15 |
ES2094734T3 (es) | 1997-02-01 |
US5306717A (en) | 1994-04-26 |
IL93908A0 (en) | 1990-12-23 |
FI93015B (fi) | 1994-10-31 |
HUT53654A (en) | 1990-11-28 |
GR3021531T3 (en) | 1997-01-31 |
HU901893D0 (en) | 1990-08-28 |
NO901418L (no) | 1990-10-01 |
ZA902381B (en) | 1990-12-28 |
DE3910093A1 (de) | 1990-10-04 |
JPH02286685A (ja) | 1990-11-26 |
IL93908A (en) | 1995-01-24 |
FI901520A0 (fi) | 1990-03-27 |
AU5232490A (en) | 1990-10-04 |
CA2013226C (en) | 2000-05-16 |
HU205122B (en) | 1992-03-30 |
DE59010527D1 (de) | 1996-11-14 |
PT93581A (pt) | 1990-11-07 |
JP2898054B2 (ja) | 1999-05-31 |
ATE143963T1 (de) | 1996-10-15 |
EP0390066A3 (de) | 1992-02-26 |
DK0390066T3 (da) | 1997-02-17 |
EP0390066A2 (de) | 1990-10-03 |
CA2013226A1 (en) | 1990-09-29 |
NO901418D0 (no) | 1990-03-28 |
AU619395B2 (en) | 1992-01-23 |
EP0390066B1 (de) | 1996-10-09 |
FI93015C (fi) | 1995-02-10 |
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